Need for the Assessment and Consultation Team (ACT) Following Anesthetic Care

Sponsor
Nationwide Children's Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02754947
Collaborator
(none)
100
1
12.9
7.7

Study Details

Study Description

Brief Summary

The goal of this study was to identify the etiology of events and demographics of patients that experience complications requiring activation of the Rapid Response Team (RRT) during the first 24 h following anesthetic care.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    100 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Etiology of Post-anesthetic and Post-sedation Events on the Inpatient Ward: Data From a Rapid Response Team at a Tertiary Care Children's Hospital
    Study Start Date :
    Feb 1, 2015
    Actual Primary Completion Date :
    Feb 1, 2016
    Actual Study Completion Date :
    Mar 1, 2016

    Outcome Measures

    Primary Outcome Measures

    1. Identifying post-operative criteria for activation of Rapid Response Teams (RRTs) in caring for the pediatric population using Pediatric Early Warning Scores (PEWS) [24 hours post-operatively]

      To retrospectively identify the etiologies associated with a need to engage Rapid Response Teams (RRTs) to promote frequent assessments and early interventions among clinically deteriorating hospitalized pediatric patients.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Any study subject that experienced an ACT following anesthetic administration during care at any Nationwide Children's Hospital facility.
    Exclusion Criteria:
    • Any study subject that has not experienced an ACT following anesthetic administration during care at any Nationwide Children's Hospital facility.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Nationwide Children's Hospital Columbus Ohio United States 43205

    Sponsors and Collaborators

    • Nationwide Children's Hospital

    Investigators

    • Principal Investigator: N'Diris Barry, BS, RN, MSN, Nationwide Children's Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    N'Diris (SAM) Barry, RN Clinical Research Coordinator, Nationwide Children's Hospital
    ClinicalTrials.gov Identifier:
    NCT02754947
    Other Study ID Numbers:
    • IRB14-00946
    First Posted:
    Apr 28, 2016
    Last Update Posted:
    Apr 6, 2017
    Last Verified:
    Apr 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by N'Diris (SAM) Barry, RN Clinical Research Coordinator, Nationwide Children's Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 6, 2017